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- Publisher Website: 10.1016/S0021-9150(96)06015-7
- Scopus: eid_2-s2.0-0031041840
- PMID: 9069518
- WOS: WOS:A1997WX81300009
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Article: LDL subfractions in acromegaly: Relation to growth hormone and insulin-like growth factor-I
Title | LDL subfractions in acromegaly: Relation to growth hormone and insulin-like growth factor-I |
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Authors | |
Keywords | acromegaly cholesteryl ester transfer protein growth hormone hepatic lipase insulin-like growth factor-I lipoprotein lipase small dense low density lipoprotein |
Issue Date | 1997 |
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/atherosclerosis |
Citation | Atherosclerosis, 1997, v. 129 n. 1, p. 59-65 How to Cite? |
Abstract | Acromegaly is associated with changes in lipoprotein metabolism and an excess in cardiovascular mortality. We have examined low density lipoprotein (LDL) subfraction distribution in 24 patients with active acromegaly and in controls matched for age, sex and body mass index. LDL was subfractionated by density gradient ultracentrifugation. The concentration of small dense LDL-III was significantly higher in the acromegalic patients compared to the controls (94.2 + 44.9 versus 67.2 + 30.4 mg/dl, P < 0.05) and there was a concomitant reduction in the intermediate subfraction LDL-II (124.8 + 31.3 versus 149.9 + 30.0 mg/dl, P < 0.05). Univariate analysis showed that both growth hormone (GH) and insulin-like growth factor (IGF)-I correlated with LDL-III and inversely with LDL-II. Acromegalic patients were found to have lower hepatic lipase (HL) and lipoprotein lipase (LPL) activities than controls (HL: 13.29 + 6.56 versus 21.58 + 7.27 μmol FFA released/ml/h, P < 0.001; LPL: 7.22 + 3.04 versus 11.53 + 7.85 μmol FFA released/ml/h, P < 0.05) whereas plasma cholesteryl ester transfer protein (CETP) activity was significantly increased (8.15 ± 1.81 versus 5.54 ± 1.86 pmol/μl/h, P < 0.001). Both GH and IGF-I were significantly associated with HL, LPL and CETP activities. Multivariate analysis on this relatively small sample size showed that in normal subjects, triglyceride and HL activity were the major determinants of LDL-III. In contrast, GH and HDL were the main determinants in acromegaly, accounting for 32 and 24% in the variability of LDL-III respectively. In conclusion, GH excess has a direct effect on LDL subfraction distribution. |
Persistent Identifier | http://hdl.handle.net/10722/78271 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.461 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tan, KCB | en_HK |
dc.contributor.author | Shiu, SWM | en_HK |
dc.contributor.author | Janus, ED | en_HK |
dc.contributor.author | Lam, KSL | en_HK |
dc.date.accessioned | 2010-09-06T07:41:02Z | - |
dc.date.available | 2010-09-06T07:41:02Z | - |
dc.date.issued | 1997 | en_HK |
dc.identifier.citation | Atherosclerosis, 1997, v. 129 n. 1, p. 59-65 | en_HK |
dc.identifier.issn | 0021-9150 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/78271 | - |
dc.description.abstract | Acromegaly is associated with changes in lipoprotein metabolism and an excess in cardiovascular mortality. We have examined low density lipoprotein (LDL) subfraction distribution in 24 patients with active acromegaly and in controls matched for age, sex and body mass index. LDL was subfractionated by density gradient ultracentrifugation. The concentration of small dense LDL-III was significantly higher in the acromegalic patients compared to the controls (94.2 + 44.9 versus 67.2 + 30.4 mg/dl, P < 0.05) and there was a concomitant reduction in the intermediate subfraction LDL-II (124.8 + 31.3 versus 149.9 + 30.0 mg/dl, P < 0.05). Univariate analysis showed that both growth hormone (GH) and insulin-like growth factor (IGF)-I correlated with LDL-III and inversely with LDL-II. Acromegalic patients were found to have lower hepatic lipase (HL) and lipoprotein lipase (LPL) activities than controls (HL: 13.29 + 6.56 versus 21.58 + 7.27 μmol FFA released/ml/h, P < 0.001; LPL: 7.22 + 3.04 versus 11.53 + 7.85 μmol FFA released/ml/h, P < 0.05) whereas plasma cholesteryl ester transfer protein (CETP) activity was significantly increased (8.15 ± 1.81 versus 5.54 ± 1.86 pmol/μl/h, P < 0.001). Both GH and IGF-I were significantly associated with HL, LPL and CETP activities. Multivariate analysis on this relatively small sample size showed that in normal subjects, triglyceride and HL activity were the major determinants of LDL-III. In contrast, GH and HDL were the main determinants in acromegaly, accounting for 32 and 24% in the variability of LDL-III respectively. In conclusion, GH excess has a direct effect on LDL subfraction distribution. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/atherosclerosis | en_HK |
dc.relation.ispartof | Atherosclerosis | en_HK |
dc.rights | Atherosclerosis. Copyright © Elsevier Ireland Ltd. | en_HK |
dc.subject | acromegaly | - |
dc.subject | cholesteryl ester transfer protein | - |
dc.subject | growth hormone | - |
dc.subject | hepatic lipase | - |
dc.subject | insulin-like growth factor-I | - |
dc.subject | lipoprotein lipase | - |
dc.subject | small dense low density lipoprotein | - |
dc.subject.mesh | Acromegaly - blood - drug therapy | en_HK |
dc.subject.mesh | Apolipoproteins - blood | en_HK |
dc.subject.mesh | Biological Markers - blood | en_HK |
dc.subject.mesh | Body Mass Index | en_HK |
dc.subject.mesh | Bromocriptine - therapeutic use | en_HK |
dc.subject.mesh | Carrier Proteins - blood | en_HK |
dc.subject.mesh | Cholesterol Ester Transfer Proteins | en_HK |
dc.subject.mesh | Cholesterol, HDL - blood | en_HK |
dc.subject.mesh | Fatty Acids, Nonesterified - blood | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Glycoproteins | en_HK |
dc.subject.mesh | Growth Hormone - blood - drug effects | en_HK |
dc.subject.mesh | Hormone Antagonists - therapeutic use | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Insulin-Like Growth Factor I - drug effects - metabolism | en_HK |
dc.subject.mesh | Lipase - blood | en_HK |
dc.subject.mesh | Lipoprotein Lipase - blood | en_HK |
dc.subject.mesh | Lipoproteins, LDL - blood - drug effects | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Radioimmunoassay | en_HK |
dc.subject.mesh | Risk Factors | en_HK |
dc.subject.mesh | Triglycerides - blood | en_HK |
dc.title | LDL subfractions in acromegaly: Relation to growth hormone and insulin-like growth factor-I | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0021-9150&volume=129&spage=59&epage=65&date=1997&atitle=LDL+subfractions+in+acromegaly:+relation+to+growth+hormone+and+insulin-like+growth+factor-I | en_HK |
dc.identifier.email | Tan, KCB:kcbtan@hku.hk | en_HK |
dc.identifier.email | Lam, KSL:ksllam@hku.hk | en_HK |
dc.identifier.authority | Tan, KCB=rp00402 | en_HK |
dc.identifier.authority | Lam, KSL=rp00343 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/S0021-9150(96)06015-7 | en_HK |
dc.identifier.pmid | 9069518 | en_HK |
dc.identifier.scopus | eid_2-s2.0-0031041840 | en_HK |
dc.identifier.hkuros | 22822 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0031041840&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 129 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 59 | en_HK |
dc.identifier.epage | 65 | en_HK |
dc.identifier.isi | WOS:A1997WX81300009 | - |
dc.publisher.place | Ireland | en_HK |
dc.identifier.scopusauthorid | Tan, KCB=8082703100 | en_HK |
dc.identifier.scopusauthorid | Shiu, SWM=7005550652 | en_HK |
dc.identifier.scopusauthorid | Janus, ED=7006936536 | en_HK |
dc.identifier.scopusauthorid | Lam, KSL=8082870600 | en_HK |
dc.identifier.issnl | 0021-9150 | - |